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FDA 510(k)

SPETZLER SCALP RETRACTOR CLAMPS (VARIOUS STYLES AND SIZES)

K-Number: K090272 · 2009-03-18

Decision Date2009-03-18
Product CodeGZT
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SPETZLER SCALP RETRACTOR CLAMPS (VARIOUS STYLES AND SIZES) is the device name listed in this FDA 510(k) record. The listed applicant is Cardinal Health, Inc.. It received FDA 510(k) clearance on 2009-03-18 under 510(k) number K090272. The device is classified under product code GZT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPETZLER SCALP RETRACTOR CLAMPS (VARIOUS STYLES AND SIZES)?

SPETZLER SCALP RETRACTOR CLAMPS (VARIOUS STYLES AND SIZES) is a medical device that received FDA 510(k) clearance on 2009-03-18. The listed applicant is Cardinal Health, Inc.. The 510(k) number is K090272.

When did SPETZLER SCALP RETRACTOR CLAMPS (VARIOUS STYLES AND SIZES) receive FDA 510(k) clearance?

SPETZLER SCALP RETRACTOR CLAMPS (VARIOUS STYLES AND SIZES) received FDA 510(k) clearance on 2009-03-18, under 510(k) number K090272.

Who is the listed applicant for SPETZLER SCALP RETRACTOR CLAMPS (VARIOUS STYLES AND SIZES)?

The FDA 510(k) record lists Cardinal Health, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPETZLER SCALP RETRACTOR CLAMPS (VARIOUS STYLES AND SIZES)?

The FDA product code for SPETZLER SCALP RETRACTOR CLAMPS (VARIOUS STYLES AND SIZES) is GZT.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Cardinal Health, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 26 devices →

Related Devices (Code: GZT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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